The visible electronic spectral behaviour of Eriochrome Black T, in a
number of organic solvents of different characteristics has been exami
ned. It was concluded that the dye exists in solution in basic solvent
s (based on their autoprotolysis constant, pK(s)) in an azo reversible
arrow hydrazone tautomeric equilibrium, while in acetone, acetonitril
e and DMSO it exists mainly in the azo form. In DMF and other basic so
lvent solutions, the dye exhibits an acid-base equilibrium of the type
H2In- reversible arrow HIn2- + H-2. The proportional concentration of
the base form (HIn2-), as well as the relative tautomerisation, are l
argely dependent upon the concentration of Erio T, the basicity of the
solvent and the tendency of the base and/or the hydrazone form to be
stabilized by H-bonding interaction with the solvent molecules. The co
mpound wasfound to aggr-egate in wafer and hydroxylic solvents. The ba
nds displayed by the difSerents forms of the compound have been assign
ed to an electronic transition involving the whole molecule with an ap
preciable clzalge transfer character.